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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1004062Generated: October 30, 2026

Ethyl chloroformate → ethyl 2-acetyl-6-methoxy-1-methyl-2,3,4,9-tetrahydro-1H-beta-carboline-9-carboxylate

https://huagongshe.com/reaction/1004062

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 18328986HCID 18328986—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventDichloromethaneHCID 6344—
Productethyl 2-acetyl-6-methoxy-1-methyl-2,3,4,9-tetrahydro-1H-beta-carboline-9-carboxylateHCID 1879421670%

Reaction Steps

Sodium hydroxide (3 g), tetrabutylammonium hydrogen sulphate (1.87 g) and ethyl chloroformate (2.2 mL) are successively added to a solution of 1-(6-methoxy- 1-methyl-2,3,4,9-tetrahydro-1H-β-carbolin-2-yl)-1-ethanone (1.45 g) in dichloromethane (100 mL). The mixture is stirred at room temperature for 3 h. After separation on silica gel (chloroform/methanol eluent), the ethyl 2-acetyl-6-methoxy-1 -methyl-2,3,4,9-tetrahydro-1H-β-carboline-9-carboxylate is obtained (70% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06048868
Source datasetuspto-grants-2000_04
ORD IDord-0e949290e988481d916e0685d660a6f3
Source noteuspto-grants-2000_04